J. S. Bamforth

发表

Use of Magnetic Resonance Imaging to Measure Facial Soft Tissue Depth

J. V. Pluym, W. W. Shan, Z. Taher, 2007, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Assessment of soft tissue facial asymmetry in medically normal and syndrome-affected individuals by analysis of landmarks and measurements.

A E Peterson, A. Peterson, O. B. Beattie, 2000, American journal of medical genetics.

Cold-induced sweating syndrome: CISS1 and CISS2 Manifestations from infancy to adulthood. Four new cases

J. Mcleod, J. Miles, A. Hahn, 2010, Journal of the Neurological Sciences.

Differential CRX and OTX2 expression in human retina and retinoblastoma

R. Godbout, D. Glubrecht, J. S. Bamforth, 2009, Journal of neurochemistry.

Anthropometry of Soft Facial Tissues

J. S. Bamforth, J. Bamforth, 2012 .

Polytopic anomalies with agenesis of the lower vertebral column.

E. Zackai, J. Opitz, S. Mundlos, 1999, American journal of medical genetics.

Maternal uniparental heterodisomy for chromosome 16: case report.

P. Bridge, J. S. Bamforth, V. Woo, 1997, American journal of medical genetics.

Genetic study of SOX9 in a case of campomelic dysplasia.

M. Walter, J. S. Bamforth, J. Giordano, 2001, American journal of medical genetics.

Soft tissue facial resemblance in families and syndrome-affected individuals.

A E Peterson, A. Peterson, O. B. Beattie, 2001, American journal of medical genetics.

Facial measurements in clinical genetics: How important are the instruments we use?

A. Peterson, O. B. Beattie, J. S. Bamforth, 1998, American journal of medical genetics.

Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.

P. Kaurah, J. S. Bamforth, 1992, American journal of medical genetics.

Amniotic band sequence: Streeter's hypothesis reexamined.

J. S. Bamforth, J. Bamforth, 1992, American journal of medical genetics.

X-linked situs abnormalities result from mutations in ZIC3

D. Schlessinger, D. Nelson, M. Gebbia, 1997, Nature Genetics.

Adams Oliver syndrome: a family with extreme variability in clinical expression.

P. Kaurah, J. S. Bamforth, J. Byrne, 1994, American journal of medical genetics.

Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease

M. Somerville, J. S. Bamforth, J. Dyck, 2004, Circulation research.

Poland anomaly with a limb body wall disruption defect: case report and review.

G. Machin, L. Honoré, J. S. Bamforth, 1992, American journal of medical genetics.

Structural anomalies in patients with inherited metabolic diseases

D. Applegarth, J. S. Bamforth, F. Bamforth, 1994, Journal of Inherited Metabolic Disease.

Disruption sequences: embryonic vascular accident or blastogenic disruption sequence?

J. S. Bamforth, J. Bamforth, 1993, American journal of medical genetics.

Technical note: Different techniques, different results--a comparison of photogrammetric and caliper-derived measurements.

A. Peterson, O. B. Beattie, J. S. Bamforth, 1998, American journal of physical anthropology.